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Senior Director, Global Oncology Therapeutic Area Safety Physician, Cambridge
Client:
Gilead Sciences International, Ltd. Location:
Cambridge, United Kingdom Job Category:
Other EU work permit required:
Yes Job Reference:
087f693c3aa8 Job Views:
81 Posted:
22.01.2025 Expiry Date:
08.03.2025 Job Description:
Description Serves as a senior scientific and clinical expert for safety profile of products in therapeutic areas. Defines global product safety strategy and routinely manages and leads functional and cross-functional projects. Works under consultative direction towards long-term GLPS goals and objectives; assignments are self-initiated with almost no direct supervision. Serves on senior-level cross-functional teams. Communicates to highest levels of senior management key pharmacovigilance findings. Provides global medical leadership for product-focused safety activities. Provides global strategic input to the organization to mitigate pharmacovigilance-related risk. Executes process changes and initiatives based on deep understanding of good pharmacovigilance practices (GVP) and other regulatory guidance. Participates in standard operating procedure (SOP) updates, audits, data analysis, and other ad hoc activities. Collaborates with Medical Safety Science- Global TA Safety Scientists in proactive identification and assessment of safety signals and trends, and supports management of any potential safety issues. Essential Duties: Oversees clinical development and medical safety support for all project-related activities for multiple products. Provides medical strategy and input into key regulatory decisions pertaining to the safety of multiple products, including representing the GLPS Department at advisory panels and meetings with regulators or other internal and external stakeholders. Establishes the direction of pharmacovigilance activities for assigned products and provides global medical leadership and input into all aspects of safety of assigned molecules within the Oncology TA including surveillance programs, aggregate review, and risk management planning. Leads a portion of BLA submission activities. Requirements: MD/DO/Pharm D degree or equivalent. Completion of an accredited medical or surgical residency program is required. Board certification is preferred. 6+ years (with MD or PharmD) in pharmacovigilance, drug development or applicable role in the pharmaceutical industry with significant knowledge of relevant regulatory requirements and substantial knowledge of drug safety including previous experience in a leadership role in the pharmaceutical industry. Experience in Hematology/Oncology/Immunology is preferred. Experience in a basic science laboratory and/or proficiency in translational research is preferred. Experience in submission of BLA/NDA is preferred. Demonstrates an excellent scientific/clinical and analytical knowledge base, with ability to assess data and understand the safety/medical implications. Possesses significant knowledge of EU and FDA pharmacovigilance guidelines, good clinical practice (GCP), and clinical research methodology. Establishes recognition as a clinical and scientific expert on project and cross-functional teams and “end-line” decision maker for product safety decisions on behalf of GLPS. Demonstrates ability to independently lead crisis management scenarios. Demonstrates ability to self-initiate pharmacovigilance processes. Equal Employment Opportunity (EEO) It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual’s gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws. For Current Gilead Employees and Contractors: Please log onto your to apply for this job.
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Client:
Gilead Sciences International, Ltd. Location:
Cambridge, United Kingdom Job Category:
Other EU work permit required:
Yes Job Reference:
087f693c3aa8 Job Views:
81 Posted:
22.01.2025 Expiry Date:
08.03.2025 Job Description:
Description Serves as a senior scientific and clinical expert for safety profile of products in therapeutic areas. Defines global product safety strategy and routinely manages and leads functional and cross-functional projects. Works under consultative direction towards long-term GLPS goals and objectives; assignments are self-initiated with almost no direct supervision. Serves on senior-level cross-functional teams. Communicates to highest levels of senior management key pharmacovigilance findings. Provides global medical leadership for product-focused safety activities. Provides global strategic input to the organization to mitigate pharmacovigilance-related risk. Executes process changes and initiatives based on deep understanding of good pharmacovigilance practices (GVP) and other regulatory guidance. Participates in standard operating procedure (SOP) updates, audits, data analysis, and other ad hoc activities. Collaborates with Medical Safety Science- Global TA Safety Scientists in proactive identification and assessment of safety signals and trends, and supports management of any potential safety issues. Essential Duties: Oversees clinical development and medical safety support for all project-related activities for multiple products. Provides medical strategy and input into key regulatory decisions pertaining to the safety of multiple products, including representing the GLPS Department at advisory panels and meetings with regulators or other internal and external stakeholders. Establishes the direction of pharmacovigilance activities for assigned products and provides global medical leadership and input into all aspects of safety of assigned molecules within the Oncology TA including surveillance programs, aggregate review, and risk management planning. Leads a portion of BLA submission activities. Requirements: MD/DO/Pharm D degree or equivalent. Completion of an accredited medical or surgical residency program is required. Board certification is preferred. 6+ years (with MD or PharmD) in pharmacovigilance, drug development or applicable role in the pharmaceutical industry with significant knowledge of relevant regulatory requirements and substantial knowledge of drug safety including previous experience in a leadership role in the pharmaceutical industry. Experience in Hematology/Oncology/Immunology is preferred. Experience in a basic science laboratory and/or proficiency in translational research is preferred. Experience in submission of BLA/NDA is preferred. Demonstrates an excellent scientific/clinical and analytical knowledge base, with ability to assess data and understand the safety/medical implications. Possesses significant knowledge of EU and FDA pharmacovigilance guidelines, good clinical practice (GCP), and clinical research methodology. Establishes recognition as a clinical and scientific expert on project and cross-functional teams and “end-line” decision maker for product safety decisions on behalf of GLPS. Demonstrates ability to independently lead crisis management scenarios. Demonstrates ability to self-initiate pharmacovigilance processes. Equal Employment Opportunity (EEO) It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual’s gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws. For Current Gilead Employees and Contractors: Please log onto your to apply for this job.
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